Canonical Allele Identifier: CA2461412172

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561782C= , CM000685.2:g.139561782C=	GRCh38
NC_000023.10:g.138643941C= , CM000685.1:g.138643941C=	GRCh37
NC_000023.9:g.138471607C=	NCBI36
NG_007994.1:g.36047C= , LRG_556:g.36047C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1097C= MANE Select	ENSP00000218099.2:p.Ala366=
ENST00000643157.1:n.1723+41C=
ENST00000218099.6:c.1097C=	ENSP00000218099.2:p.Ala366=
ENST00000394090.2:c.983C=	ENSP00000377650.2:p.Ala328=
NM_000133.3:c.1097C= , LRG_556t1:c.1097C=	NP_000124.1:p.Ala366=
NM_001313913.1:c.983C=	NP_001300842.1:p.Ala328=
XM_005262397.3:c.968C=	XP_005262454.1:p.Ala323=
XM_005262397.4:c.968C=	XP_005262454.1:p.Ala323=
NM_000133.4:c.1097C= MANE Select	NP_000124.1:p.Ala366=
NM_001313913.2:c.983C=	NP_001300842.1:p.Ala328=